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what happens when n-butyl bromide is Treated Aqueous KOH and why ?
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but SN2 proceeds in non-polar solvents o.O
SN2 proceeds in Polar aprotic solvents where as water is a polar protic solvent
The SN1 is favoured by stabilizing the bromide ion
but how can the carbocation is stablized in SN1 it is a primary alkyl halide ?
it's likely that there is a hydride shift from one of the carbons beside it, making it a secondary carbocation.
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